Accurate Diagnosis of Pseudomonas aeruginosa Is Critical to Mitigating Development of Antibiotic Resistance.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES
Hala I Al-Daghistani, Lubna F Abu-Niaaj, Sima Zein
{"title":"Accurate Diagnosis of <i>Pseudomonas aeruginosa</i> Is Critical to Mitigating Development of Antibiotic Resistance.","authors":"Hala I Al-Daghistani, Lubna F Abu-Niaaj, Sima Zein","doi":"10.3390/antibiotics14050509","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background</b>: The accurate and rapid diagnosis of infections is critical for effective and timely treatment. Misdiagnosis often leads to the prescription of antibiotics not targeting the causing agent of infection and thus be the possible development of multidrug resistance. This collectively worsens the condition and might lead to unnecessary intervention or death. The abundance of <i>Pseudomonas</i> spp. in healthcare-settings and the environment may lead to the inaccurate diagnosis of <i>P. aeruginosa</i>, making the treatment of its infections challenging. <i>P. aeruginosa</i> is a Gram-negative, opportunistic pathogen commonly linked to healthcare-associated infections. Its pathogenicity is attributed to several virulence factors correlated to enhanced survivability and colonization, invasion of the host tissues, and the development of multidrug resistance. When advanced diagnostic facilities are limited or unaffordable, the prescription of antibiotics solely relies on identifying the bacteria by culture-based methods. <b>Objectives</b>: This study aims to validate the accuracy of diagnosis of fifty clinical isolates preidentified as <i>P. aeruginosa</i> in three healthcare facilities in Jordan. <b>Methods</b>: The isolates were from infected areas of patients, including skin, wounds, ears, urine, and peritoneal cavities. Morphological and biochemical tests were performed, and the validation relied on the polymerase chain reaction (PCR) amplification of the 16S ribosomal ribonucleic acid (rRNA) gene. This molecular method is affordable for medical facilities with limited finances in contrast to advanced high-cost techniques. <b>Results</b>: The PCR confirmed that only 60% of the isolates were <i>P. aeruginosa</i>. All the confirmed isolates could produce different pigments and form biofilms. <b>Conclusions</b>: The high percentage of isolates mistakenly identified as <i>P. aeruginosa</i> raises concern about the suitability of prescribed antibiotics. The present study strongly recommends using advanced molecular methods to identify the pathogens. If conventional methods remain the only diagnostic option, this study recommends frequent external validation for tests in addition to performing an antibiotic susceptibility test to pinpoint the effective antibiotics against biofilm-producing <i>P. aeruginosa.</i></p>","PeriodicalId":54246,"journal":{"name":"Antibiotics-Basel","volume":"14 5","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12108264/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antibiotics-Basel","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/antibiotics14050509","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The accurate and rapid diagnosis of infections is critical for effective and timely treatment. Misdiagnosis often leads to the prescription of antibiotics not targeting the causing agent of infection and thus be the possible development of multidrug resistance. This collectively worsens the condition and might lead to unnecessary intervention or death. The abundance of Pseudomonas spp. in healthcare-settings and the environment may lead to the inaccurate diagnosis of P. aeruginosa, making the treatment of its infections challenging. P. aeruginosa is a Gram-negative, opportunistic pathogen commonly linked to healthcare-associated infections. Its pathogenicity is attributed to several virulence factors correlated to enhanced survivability and colonization, invasion of the host tissues, and the development of multidrug resistance. When advanced diagnostic facilities are limited or unaffordable, the prescription of antibiotics solely relies on identifying the bacteria by culture-based methods. Objectives: This study aims to validate the accuracy of diagnosis of fifty clinical isolates preidentified as P. aeruginosa in three healthcare facilities in Jordan. Methods: The isolates were from infected areas of patients, including skin, wounds, ears, urine, and peritoneal cavities. Morphological and biochemical tests were performed, and the validation relied on the polymerase chain reaction (PCR) amplification of the 16S ribosomal ribonucleic acid (rRNA) gene. This molecular method is affordable for medical facilities with limited finances in contrast to advanced high-cost techniques. Results: The PCR confirmed that only 60% of the isolates were P. aeruginosa. All the confirmed isolates could produce different pigments and form biofilms. Conclusions: The high percentage of isolates mistakenly identified as P. aeruginosa raises concern about the suitability of prescribed antibiotics. The present study strongly recommends using advanced molecular methods to identify the pathogens. If conventional methods remain the only diagnostic option, this study recommends frequent external validation for tests in addition to performing an antibiotic susceptibility test to pinpoint the effective antibiotics against biofilm-producing P. aeruginosa.

准确诊断铜绿假单胞菌对减轻抗生素耐药性至关重要。
背景:准确、快速诊断感染是有效、及时治疗的关键。误诊往往导致抗生素的处方不针对引起感染的病原体,从而有可能发展为多药耐药。这些共同使病情恶化,并可能导致不必要的干预或死亡。卫生保健机构和环境中假单胞菌的丰富可能导致铜绿假单胞菌的不准确诊断,使其感染的治疗具有挑战性。铜绿假单胞菌是一种革兰氏阴性的机会性病原体,通常与卫生保健相关感染有关。其致病性归因于几种毒力因素,这些毒力因素与增强的生存能力和定植、入侵宿主组织以及多药耐药性的发展有关。当先进的诊断设备有限或负担不起时,抗生素的处方仅依赖于通过基于培养的方法识别细菌。目的:本研究旨在验证50临床分离预先确定为铜绿假单胞菌在约旦三个医疗机构的诊断准确性。方法:从患者皮肤、创面、耳部、尿液、腹膜腔等感染部位分离。形态学和生化测试,验证依赖于16S核糖体核糖核酸(rRNA)基因的聚合酶链反应(PCR)扩增。与先进的高成本技术相比,这种分子方法对于资金有限的医疗机构来说负担得起。结果:经PCR鉴定,铜绿假单胞菌的分离率仅为60%。所有确认的分离株均能产生不同的色素并形成生物膜。结论:较高比例的分离株被误认为铜绿假单胞菌,引起了对处方抗生素适用性的关注。本研究强烈建议使用先进的分子方法来鉴定病原体。如果传统方法仍然是唯一的诊断选择,本研究建议除了进行抗生素敏感性试验以确定对产生生物膜的铜绿假单胞菌有效的抗生素外,还要经常进行外部验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信